Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective study by Nan Guo, Huili Xue, Bin Liang, Hailong Huang, Meiying Cai, Liangpu Xu

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Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective c... by Meiying Cai, Aixiang Lv, Wantong Zhao, Liangpu Xu, Na Lin, Hailong Huang

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Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome by Meiying Cai, Min Lin, Nan Guo, Meimei Fu, Liangpu Xu, Na Lin, Hailong Huang

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Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis by Xiaorui Xie, Baojia Huang, Linjuan Su, Meiying Cai, Yuqin Chen, Xiaoqing Wu, Liangpu Xu

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Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers by Meiying Cai, Na Lin, Xuemei Chen, Meimei Fu, Nan Guo, Liangpu Xu, Hailong Huang

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16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up by Meiying Cai, Yanting Que, Xuemei Chen, Yuqing Chen, Bin Liang, Hailong Huang, Liangpu Xu, Na Lin

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Fetal Aberrant Right Subclavian Artery: Associated Anomalies, Genetic Etiology, and Postnatal Outcomes in a Retrospective Cohort Study by Meiying Cai, Na Lin, Xiangqun Fan, Xuemei Chen, Shiyi Xu, Xianguo Fu, Liangpu Xu, Hailong Huang

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Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis in southern China: a retrospective analysis by Meiying Cai, Nan Guo, Meimei Fu, Yuqing Chen, Bin Liang, Yanting Que, Qingqiang Ji, Hailong Huang, Liangpu Xu, Na Lin

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Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study by Yanting Que, Meiying Cai, Fang Yang, Qingqiang Ji, Shuqi Zhang, Wenhui Huang, Yashi Gao, Bojing Zhou, Hailong Huang, Hua Cao, Na Lin

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Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios by Xiaoqing Wu, Ying Li, Na Lin, Linjuan Su, Xiaorui Xie, Bing Liang, Qingmei Shen, Meiying Cai, Danhua Guo, Hailong Huang, Liangpu Xu

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